Vous êtes sur la page 1sur 4

Science of the Total Environment 634 (2018) 497–500

Contents lists available at ScienceDirect

Science of the Total Environment

journal homepage: www.elsevier.com/locate/scitote nv

Short Communication

Soil microbial biomass: A key soil driver in management of


ecosystem functioning
Jay Shankar Singh a,⁎, Vijai Kumar Gupta b
a
Department of Environmental Microbiology, Babasaheb Bhimrao Ambedkar (Central) University, Raebarelly Road, Lucknow 226025, Uttar Pradesh, India
b
Department of Chemistry and Biotechnology, ERA Chair of Green Chemistry, School of Science, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia

HIGHLI GH T S G R A P HICAL A BS T R A C T

• Soil microbial biomass as a key ecologi- cal


driver has been described.
• Soil microbial diversity and biomass play
key roles in the ecosystem services.
• Soil micro-flora N uptake is an adapta- tion
for short-term storage of N in ter- restrial
ecosystems.
• Soil microbial biomass is key ecological
driver in rehabilitation of degraded
lands.

article i nfo abstract


Article history: Although patterns of microbial diversity and biomass have been described and reviewed at local and regional scales, a
Received 28 February 2018
unifying driver, or set of environmental drivers affecting soil microbial biomass (SMB) pattern at global level is still missing.
Received in revised form 30 March 2018
Biomass of soil microbial community, known as SMB is considered widely as the index of soil fertility and ecosystem
Accepted 30 March 2018
productivity. The escalating soil stresses due to land degradation and climatic variability are directly correlated with loss of
Available online 7 April 2018
microbial diversity and abundance or biomass dynamics. Therefore, alleviating soil stresses on microbial communities with
ecological restoration could reduce the unpredictability and turn- over rates of SMB. Thus, the key ecological factors which
Editor: Frederic Coulon
stabilize the SMB and minimize its turnover, are sup- posed to play an important role in the soil nutrient dynamics and
productivity of the ecosystems. Because of the existing public concern about the deleterious impacts of ecosystem
Keywords:
Land degradation
degradation, there is an increasing inter- est in improving the understanding of SMB, and the way, it contributes to
Environmental drivers restoration and functioning of ecosystems.
Microbial community © 2018 Elsevier B.V. All rights reserved.
Soil microbial biomass

1. Microbial biomass under different ecological regimes and ecosys- tem types microbial interactions in the soil-plant-animal food web (Seneviratne,
2015). Soil microbial diversity and abundance/biomass play key roles in the
Functioning of ecosystems rely on the flux of chemical signals, car- bon, ecosystem sustainability by maintaining essential functions of soil health,
and nutrients across the trophic levels, mainly mediated by through carbon and nutrient turnover. Even after distur- bances, an ecosystem
with a higher microbial diversity and biomass may have a higher capacity to
⁎ Corresponding author. sustain the ecological processes through microbiological buffering. There is
E-mail address: jayshankar_1@yahoo.co.in (J.S. Singh). now increasing evidence that above- ground (plant litter quantity and
quality) and belowground (soil

https://doi.org/10.1016/j.scitotenv.2018.03.373
0048-9697/© 2018 Elsevier B.V. All rights reserved.
498 J.S. Singh, V.K. Gupta / Science of the Total Environment 634 (2018) 497–500
microbial flora and fauna diversity) are key drivers that play fundamen- tal forests and mycorrhizae in boreal temperate forests) it is suggested that
roles in controlling ecosystem processes and stability (Wardle et al., variations in the size of SMB can impact to variability of the func- tioning of
2004). However, understanding ecological linkages between above- and various ecosystem types.
belowground abiotic and biotic (including SMB) attributes is still a key The rise in unpredictable climate shift and anthropogenic perturba- tions are
challenge for our knowledge on the stability and functioning of ecosystem the critical drivers to regulate the existence and survival of in- digenous
processes. Therefore, given the importance of SMB dynamics in defining microbial diversity, and consequently, the essential soil functioning of the
ecosystem properties, the understanding as to how SMB re- spond to ecosystem. The macroclimate, topography and soil quality (pH, organic C and
unexpected rise in biotic and abiotic drivers and loss of plant species diversity N, moisture, etc.) are the key drivers in con- trolling SMB dynamics across
seems a research priority that would shed light on the performance of diverse different ecosystems and locations (Wardle, 1992). The temporal dynamics of
ecosystems. SMB is likely to be the key factor in determining the extent of release of
Among the various ecological drivers, microbes (N2-fixers, P- immobilized labile nutri- ents due to microbial cell deaths, and the availability
solubilizers, growth hormone producers, etc.) and their SMB pools may of nutrients re- leased crucial to plant growth and ecosystem functioning
be considered as major ecological impetus in controlling the di- verse (Wardle,
ecosystem functions globally (Table 1). Soil carbon (C) and nitro- gen (N) 1998). The factors that provide viability to the soil microbial community
together with phosphorus (P) and soil pH are the key drivers that may limit the therefore, are assumed to enhance soil nutrient conservation in the form of
functioning of various nutrient deprived ecosystems (Bru et al., 2011; Carnicer higher SMB size owing to the reduced release of immobilized nutrients. While
et al., 2015). In strongly soil N deprived eco- systems such as Arctic and studying the effect of climatic disturbances on ecosys- tem types, we may
Alpine Tundra and Temperate forests, nutri- ents release after soil micro-flora expect SMB to have lesser temporal variability owing to lesser
(SMB) death has been pointed out as an important source of plant nutrient N disturbances.
(van der Heijden et al., 2008). So, it is suggested that uptake of N by soil Along a large geographical area, climate variability, land use types and the
micro-flora might be an adap- tation that may have developed for short-term dominant vegetation composition might be the key factors for SMB variability
storage of N in several terrestrial ecosystems, thus reducing the loss of N from across different ecosystem types. Differences in the quantity and quality of
the soil of nutri- ent poor ecosystems. It is also important to mention here that substrate (organic C and N) inputs caused by varying plant residue types (litter
the chem- ical composition of plant residues (litter and fine roots) from diverse and fine roots) and the associated nu- trient specificity can be crucial drivers to
plant species in an ecosystem could be unpredictable and therefore, dif- ferent influence the SMB across the ecosystem types. Thus, the higher SMB in
microbial communities might be evolved to decay and decom- pose the variety soil of scrub stand than other ecosystems might be attributed mainly to the
of litter types. As many microbial communities have restricted bio-geographic greater availability of organic matter via vegetation cover with giant plant
distributions (N2-fixing rhizobia in tropical species. How- ever, in case the temporal data on SMB from different
ecosystems across the globe were quantitatively analyzed, more persistent and
less dis- turbed ecosystems had higher SMB values than the most disturbed one
Table 1 (Wardle, 1998), though the temporal variability of different ecosys- tem types
Microbes as key ecological drivers regulating functioning of diverse ecosystems. was substantially comparable. This indicates that temporal SMB variability is
Source: van der Heijden et al. (2008) Ecol. Lett. 11: 296–310.
solely governed by the dominant vegetation and land use type, but the nutrient
Ecosystem type Microbes Microbial functions turnover along with other edaphic fac-
Tropical savannah, Symbiotic, free living and Support plant productivity tors can be more effective than those in regulating the temporal SMB
some grasslands and endophytic N-fixing by supplying different variability. However, it is suggested that shifts in plant species composi- tion
tropical forests bacteria limiting nutrients (N) to the during land use change, can influence the microbial community composition
plants. dynamics and SMB basically by changing soil organic nutri- ent status (Zhang
Endophytes enhance
et al., 2016). But it is still unclear as to why SMB is not so responsive to large-
growth and competitive
scale disturbance regimes, such as invasions of
ability of their host plants.
Deserts and boreal N-fixing cyanobacteria Contribute to the N alien species into new territories, climate change due to atmospheric CO2
forests economy of ecosystems via
elevation, greater soil nitrogen deposition and land use changes (Wardle et al.,
N cycling and accumulation
under extremely limited 2004), and therefore, further studies in this regard, will enhance our
N2-fixation situations. understanding about temporal microbial community com- positions and
Helps in degraded land biomass variability.
restoration. Although nutrient status, seasonality, soil factors, temperature, and
Tropical, temperate and Arbuscular mycorrhizal Enhanced P uptake of host
boreal forests, (AM), Ectomycorrhizal plant species when plant
other factors, are important drivers to control functioning of dry tropical forest
grassland and (EM) and Ericoid productivity is strongly ecosystem, SMB could be one of the vital factors affecting produc- tivity in the
savannah ecosystems mycorrhizal (ERM) fungi limited by P availability. tropical dry deciduous forests, as observed in the Vindhyan plateau (Singh et
Provide resistance to plants al., 2010). In India, the previous investigations regard- ing SMB across the
against diseases, drought and tropical dry deciduous forest ecosystems have been conducted by selecting only
other environmental stresses one or the other sites on a temporal scale, and without deciphering differences
in nutrient poor in SMB status and its role in distri-
and degraded ecosystems.
Natural ecosystems P-solubilizing bacteria May constitute up to 40% of bution and variations of the dominant vegetation composition. It may be
the cultivable population of hypothesized that alterations in soil properties due to land uses and
soil bacteria.
anthropogenic activities would correspond to differences in the SMB size and
However, significance of
turnover rates and consequently, to loss of vegetation cover and ecosystem
bacteria in natural
ecosystems is still in enigma
productivity. However, the experimental evidence for such arguments is still
and further studied are still warranted.
warranted. In nutrient poor ecosystems, SMB acts as the major reservoir of avail-
Tropical forests Nitrifying and denitrifying Indirectly reduce plant
bacteria productivity because about able nutrients, and plays very crucial roles in the survival of plants (Singh et al.,
50% of available soil N is 2016a, 2016b; Vimal et al., 2017). In the dry tropical decid- uous forest
lost from the ecosystem by ecosystem, nutrient withdrawal from the senescing leaves
nitrification and and its immobilization in the SMB has been considered as the nutrient
denitri fication processes
conserving adaptations in response to nutrient paucity, and thus SMB
J.S. Singh, V.K. Gupta / Science of the Total Environment 634 (2018) 497–
500 499
constitutes the key available nutrient source for the survival of plant SMB, an important driver of ecosystem functioning, may be consid- ered as
communities (Singh et al., 2010; Singh, 2015a, 2015b). The conversion of the sensitive key biological indicator of perturbations owing to soil
forest into cropland and savanna due to plant harvesting may result a disturbances (Zornoza et al., 2009). Research practices on degraded land
significant alterations in the size of SMB. Since, plant diversity is a key driver restoration, have mainly focused on the aboveground features with lesser
in controlling SMB (Thakur et al., 2015); any alterations in the soil properties emphasis on the belowground soil microbial processes and the patterns of
due to deforestation may have significant impact on SMB stability and its SMB, which could play a vital role in productivity of the de- rived ecosystems.
turnover rates. As plant biodiversity is projected to decline in response to The soil microbial properties between degraded and restored lands have been
global environmental change factors, we can also expect indirect effects of key compared (Bini et al., 2013; Singh, 2016), but the knowledge about key
environmental drivers on SMB status via alterations in plant community environmental drivers influencing the patterns of SMB and microbial
compositions. The increasing de- mand of agricultural land accelerates community structure during restoration, is still limited. Therefore, the study of
deforestation and consequently disturbances in SMB trends had been noted. SMB patterns and its relationship to climate and soil drivers can enhance our
Although deforestation is a common practice for the generation of agricultural understanding in rehabilita- tion of land uses like vast waste lands (e.g. spoiled
managed land- use systems, afforestation has become a much discussed topic coal mine areas). It is suggested that during restoration programs, the
in recent years (Singh et al., 2010). Therefore, we suggest that long-term belowground microbial activities and their biomass development and responses
investi- gations should be conducted on the SMB patterns, a sensitive nutrient must be con- sidered in implementation. It is proposed that restoration practices
pool that may respond to plant diversity loss compared to other envi- ronmental with mixed plant species having high biomass producing potential, can
drivers. contribute to speedy recovery of lost microbial diversity and SMB turnovers
(Singh, 2013; Araujo et al., 2013; Singh, 2014). The fast recov- ery of
microbial communities and SMB size due to mixed plantations cover (Lange et
2. Microbial biomass in restoration of degraded land soil productivity al., 2015) compared to the monoculture plantations can help in the returning of
the huge bulk of diverse types of plant- derived resources (leaf litter, fine
Restoration ecology, a somewhat new thrust research area, still needs root biomass, root exudates or rhizodeposits) and favorable soil conditions.
rigorous explorations to achieve satisfactory results (Calmon et al., 2011). As In view of these, it is rec- ommended that plant species having high biomass
the changing global climate is one of the major environ- mental challenges production effi- ciency, and favoring the establishment of beneficial
today, there is an urgent need to restore the huge de- graded land area to make microbial (mycorrhizae and nitrogen-fixers) associations, should preferably be
it cultivable for the overall sustainable agro- environmental development. Size selected during restoration programs.
of SMB can provide one of the most satisfactory estimates of the productivity Speedy recovery of soil productivity on the deforested area can be achieved
of any restored degraded land (do Couto et al., 2016). A lower ratio of SMB by afforestation of mixed plantations in association with suit- able bio-
to the total soil organic nutrients seems to indicate good strength of degraded inoculants, which can be a good microbial “booster”to enhance the SMB and
land rehabilita- tion. Consequently, the ratio of SMB to the total organic ecosystem productivity (Fig. 1). The inoculation of suitable bio-fertilizers along
nutrients may be considered as a reliable parameter for the success of degraded with mixed plantations, not only increases the pop- ulation of the microbial
land rehabilitation. The re-established SMB status and its dynamics under strains inoculated, but also enhances diversity and abundance of microbes
prevailing environmental drivers may provide valuable information about the native to the soil, through dormancy break- ing of their quiescent viable spores
restoration progress and productivity potential of derived lands for agriculture developed in response to environ- mental stresses (Seneviratne and
purposes. Kulasooriya, 2013; Singh and Strong,
2016). Thus, a combination of mixed plantation, stress-tolerant bio-

Re-vegetation of degraded land

Degraded land Crop land Forest ecosystem


Microbial flora
and fauna Nutrient
Plant litters uptake by
Root exudates plants and
Soil microbial biomass
soil
&
Solubilization micro-flora
Dissolved organic matter
Decomposition
Available nutrients

Nutrient immobilization Mineralization

Fig. 1. Schematic representation showing contribution of soil microbial biomass as source of plant available nutrients to agro- and forest ecosystems.
500 J.S. Singh, V.K. Gupta / Science of the Total Environment 634 (2018) 497–500
inoculants, and organic amendments in restoration of the degraded lands may Calmon, M., Brancalion, P.H.S., Paese, A., Aronson, J., Castro, P., Costa da Silva, S.,
offer a tripartite association to augment soil nutrient turn- overs and Rodrigues, R.R., 2011. Emerging threats and opportunities for biodiversity
consequently to reinstate productivity of stressed ecosys- tems. However, it conservation and eco- logical restoration in the Atlantic forest of Brazil. Restor. Ecol.
19, 154–158.
should be kept in mind that addition of microbial inoculants into new territories
Carnicer, J., Sardans, J., Stefanescu, C., Ubachd, A., Bartrons, M., Asensio, D., Penuelas, J.,
may greatly affect soil plant-microbe in- teractions, especially when the new 2015. Global biodiversity, stoichiometry and ecosystem function responses to
microbial species has vastly differ- ent physiological behaviours from the human-induced C–N–P imbalances. J. Plant Physiol. 172, 82–91.
indigenous micro- flora. No information is available on how addition of do Couto, G.M., Eisenhauer, N., de Oliveira, E.B., Cesarz, S., Feliciano, A.L.P., Marangon,
L.C.,
exotic soil microbial inocu- lants in association with re-vegetation of degraded
2016. Response of soil microbial biomass and activity in early restored lands in the
lands can influences the exiting native soil micro-biota, although these effects northeastern Brazilian Atlantic Forest. Restor. Ecol. 24, 609–616.
should be strongest when the alien microbial inoculants has functional van der Heijden, M.G.A., Bardgett, R.D., van Straalen, N.M., 2008. The unseen majority:
attributes that are not compatibles to the indigenous microbial species. In our soil microbes as drivers of plant diversity and productivity in terrestrial ecosystems.
opinion, the future research on SMB turnovers as affected by the key Ecol. Lett. 11, 296–310.
Lange, M., Eisenhauer, N., Sierra, C.A., Bessler, H., Engels, C., Griffiths, R.I.,
ecological drivers and its correlation with the ecosystem functioning holds
Mellado- Vazquez, P.G., Malik, A.A., Roy, J., Scheu, S., Steinbeiss, S., Thomson,
potential as the complementary criteria for evaluating the rehabil- itation B.C., Trumbore, S.E., Gleixner, G., 2015. Plant diversity increases soil microbial
progress in restoration ecology. activity and soil carbon storage. Nat. Commun. 6, 6707.
Seneviratne, G., 2015. Signal transduction in edaphic ecosystems governs sustainability.
Agric. Ecosyst. Environ. 210, 47–49.
3. Conclusions
Seneviratne, G., Kulasooriya, S.A., 2013. Reinstating soil microbial diversity in
agroecosystems: the need of the hour for sustainability and health. Agric. Ecosyst. En-
Besides the importance of physico-chemical and biological processes to viron. 164, 181–182.
maintain soil health, SMB may be the ‘keystone’ biological driver of Singh, J.S., 2013. Plant growth promoting rhizobacteria: potential microbes for sustainable
ecosystem functioning. Loss of beneficial microbial diversity and SMB agriculture. Resonance 18, 275–281.
Singh, J.S., 2014. Cyanobacteria: a vital bio-agent in eco-restoration of degraded lands and
associated to land use changes and erratic climate shifts, are the major reasons
sustainable agriculture. Clim. Change Environ. Sustain. 2, 133–137.
for deterioration of soil fertility and ecosystem productivity. Therefore, Singh, J.S., 2015a. Microbes: the chief ecological engineers in reinstating equilibrium in
researches related to plant-microbe-soil associations to com- bat problems of degraded ecosystems. Agric. Ecosyst. Environ. 203, 80–82.
soil degradation need to be performed in greater depth. Today, it is the utmost Singh, J.S., 2015b. Plant-microbe interactions: a viable tool for agricultural sustainability.
need to maintain soil health and productivity with emphasis on restoration of Appl. Soil Ecol. 92, 45–46.
Singh, J.S., 2016. Microbes play major roles in ecosystem services. Clim. Change Environ.
vast area of the degraded lands using efficient biomass producing novel plant
Sustain. 3, 163–167.
species and microbial inocu- lants. Finally, SMB is concluded to be an Singh, J.S., Strong, P.J., 2016. Biologically derived fertilizer: a multifaceted bio-tool in
important index for the soil health and environmental sustainability. methane mitigation. Ecotoxicol. Environ. Saf. 124, 67–276.
Singh, J.S., Kashyap, A.K., Singh, D.P., 2010. Microbial biomass C, N and P in disturbed
dry tropical forest soils, India. Pedosphere 20 (6), 780–788.
Acknowledgement
Singh, J.S., Abhilash, P.C., Gupta, V.K., 2016a. Agriculturally important microbes in
sustain- able food production. Trends Biotechnol. 34, 773–775.
JSS is thankful to Head, Department of Environmental Microbiology, BBA Singh, J.S., Kumar, A., Rai, A.N., Singh, D.P., 2016b. Cyanobacteria: a precious bio-
University, Lucknow, India for providing all kind of supports and the resource in agriculture, ecosystem, and environmental sustainability. Front. Microbiol. 7,
infrastructure facilities. 529. Thakur, M.P., Milcu, A., Manning, P., Niklaus, P.A., Roscher, C., Power, S., Reich,
P.B., Scheu, S., Tilman, D., Ai, F., Guo, H., Ji, R., Pierce, S., Ramirez, N.G., Richter, A.N.,
Steinauer, K., Strecker, T., Vogel, A., Eisenhauer, N., 2015. Plant diversity drives soil
References microbial bio- mass carbon in grasslands irrespective of global environmental change
factors.
Araujo, A.S.F., Cesarz, S., Leite, L.F.C., Borges, C.D., Tsai, S.M., Eisenhauer, N., 2013. Glob. Chang. Biol. 21, 4076–4085.
Soil mi- crobial properties and temporal stability in degraded and restored lands of Vimal, S.R., Singh, J.S., Arora, N.K., Singh, S., 2017. Soil-plant-microbe interactions in
northeast Brazil. Soil Biol. Biochem. 66, 175–181. stressed agriculture management: a review. Pedosphere 27, 177–192.
Bini, D., dos Santos, C.A., do Carmo, K.B., Kishino, N., Andrade, G., Zangaro, W., Wardle, D.A., 1992. A comparative assessment of factors which influence microbial bio-
Nogueira, M.A., 2013. Effects of land use on soil organic carbon and microbial mass carbon and nitrogen levels in soils. Biol. Rev. 67, 321–358.
processes associ- ated with soil health in southern Brazil. Eur. J. Soil Biol. 55, 117– Wardle, D.A., 1998. Controls of temporal variability of the soil microbial biomass: a
123. global- scale synthesis. Soil Biol. Biochem. 30 (13), 1627–1637.
Bru, D., Ramette, A., Saby, N.P., Dequiedt, S., Ranjard, L., Jolivet, C., Arrouays, D., Wardle, D.A., Bardgett, R.D., Klironomos, J.N., Setala, H., van der Putten, W.H., Wall, D.H.,
Philippot, L., 2011. Determinants of the distribution of nitrogen-cycling microbial 2004. Ecological linkages between aboveground and belowground biota. Science
communities at the landscape scale. ISME J. 5, 532–542. 304, 1629–1633.
Zhang, Q., Wu, J., Yang, F., Lei, Y., Zhang, Q., Cheng, X., 2016. Alterations in soil
microbial community composition and biomass following agricultural land use change.
Sci. Rep. 6, 36587.
Zornoza, R., Guerrero, C., Mataix-Solera, J., Scow, K.M., Arcenegui, V., Mataix-Beneyto, J.,
2009. Changes in soil microbial community structure following the abandonment of
agricultural terraces in mountainous areas of eastern Spain. Appl. Soil Ecol. 42,
315–323.

Vous aimerez peut-être aussi